HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32815Generated: October 25, 2026
4-Methylmorpholine → tert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamate
https://huagongshe.com/reaction/32815
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-4,6-dimethoxy-1,3,5-triazine | HCID 18450 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 2-Amino-1,3-thiazole-4-carboxylic acid, N-BOC protected | HCID 1502051 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | tert-Butyl (4-(methoxy(methyl)carbamoyl)thiazol-2-yl)carbamate | HCID 58604314 | 88,069.203% |
Reaction Steps
A solution of 2-tert-butoxycarbonylamino-thiazole-4-carboxylic acid (14 g, 0.0573 mol), 2-chloro-4,6-dimethoxy-1,3,5-triazine (10.06 g, 0.0573 mol) and N-methyl morpholine (5.79 g, 0.0573 mol) in tetrahydrofuran was stirred for 2 hours at room temperature. N,O-Dimethylhydroxylamine hydrochloride (5.59 g, 0.0573 mmol) and triethylamine (5.59 g, 0.0573 mol) were added and the mixture was stirred for 3 days. The reaction mixture was evaporated and ethyl acetate was added. The reaction mixture was washed with 1 N aqueous hydrochloric acid and then washed with saturated aqueous sodium bicarbonate. [4-(Methoxy-methyl-carbamoyl)-thiazol-2-yl]-carbamic acid tert-butyl ester (14.5 g, 88%) was obtained as a tan tar after drying (magnesium sulfate) and evaporation.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07427635B2 |
|---|
| Source dataset | uspto-grants-2008_09 |
|---|
| ORD ID | ord-59be9c7ae1d246e5bf7b527b4f99c272 |
|---|
| Source note | uspto-grants-2008_09 |
|---|