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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480093Generated: October 25, 2026

Triethylamine → tert-Butyl 3-(methylcarbamoyl)pentan-3-ylcarbamate

https://huagongshe.com/reaction/1480093

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant2-[(tert-Butoxycarbonyl)amino]-2-ethylbutanoic acidHCID 15108504—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 3-(methylcarbamoyl)pentan-3-ylcarbamateHCID 8667475445%

Reaction Steps

A mixture of 2-(tert-butoxycarbonylamino)-2-ethylbutanoic acid (Example 45a, 400 mg, 2 mmol), HBTU (CAN 94790-37-1, 1.3 g, 3 mmol), triethylamine (0.7 g, 7 mmol) in DMF (10 mL) was stirred for 30 min, then methanamine hydrochloride (CAN 593-51-1, 260 mg, 6 mmol) was added into the mixture and the solution was stirred overnight. After that, the solution was diluted with water (20 mL) and extracted with ethyl acetate (3×30 mL), the combined organic layer was washed with water (3×50 mL) and brine (60 mL), then evaporated to dryness. The crude product (0.18 g, 45%) obtained as a light yellow solid was used for the next step directly without any purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-4ffd4c8182ae417b8d8a6f90b2f4a063
Source noteuspto-grants-2016_08