HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Thiazole-2-carboximidamide hydrochloride → 4-Cyclopropyl-thiazole-2-carboxamidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Thiazole-2-carboximidamide hydrochloride | HCID 18679584 | — |
| Reactant | 4-Cyclopropylthiazole-2-carbonitrile | HCID 71748573 | — |
| Product | 4-Cyclopropyl-thiazole-2-carboxamidine | HCID 90000916 | — |
Reaction Steps
Compound M was prepared in analogy to thiazole-2-carboxamidine (Compound A1) with the procedure shown in Scheme 5 by using 4-cyclopropyl-thiazole-2-carbonitrile instead of thiazole-2-carbonitrile. 1H NMR (CDCl3-d, 400 MHz): δ 9.68 (br, 1H), 9.56 (br, 1H), 2.23-2.19 (m, 1H), 1.01-0.92 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447086B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-667638fcd2214222959aa2d16d018834 |
| Source note | uspto-grants-2016_09 |