Tert-Butylamine → Boc-Hyp-NH-tBu
반응식
[C:1]([N:8]1[CH2:16][C@H:14]([OH:15])[CH2:13][C@H:9]1[C:10]([OH:12])=O)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:17]([NH2:21])([CH3:20])([CH3:19])[CH3:18].C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl>ClCCl>[N:8]1([C:1]([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])=[O:2])[CH2:16][C@H:14]([OH:15])[CH2:13][C@H:9]1[C:10]([NH:21][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:12]참가 물질
6
반응물 4
생성물 1
시약·촉매·용매 1
실험 절차
In a dichloromethane solution containing 5.1 g of N-Boc-hydroxyproline (Boc-Hyp-OH), 0.35 g of tert-butylamine, 7.4 g of HOBt and 6.0 g of EDC hydrochloride were added under ice cooling and the resultant mixture was stirred overnight at room temperature. The reaction mixture was treated similarly to that in Example 144 (Process 2) to give 2.59 g of the title compound.
후처리
- additionwere added under ice cooling
- additionThe reaction mixture was treated similarly to that in Example 144 (Process 2)
출처 및 근거
- ORD 기록
- ord-1b10a96c5e5d43d99a4e3cf4b8a38248
- 출처 데이터셋
- uspto-grants-2001_11
- 특허 번호
- US06313094B1
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